A Retrospective Study to Evaluate the Effectiveness of onabotulinumtoxinA in Preventing Headaches in Patients With Chronic Migraines

NCT ID: NCT01749423

Last Updated: 2014-02-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2012-11-30

Study Completion Date

2013-12-31

Brief Summary

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This study will evaluate the effectiveness of OnabotulinumtoxinA to prevent headaches in patients with Chronic Migraine.

Detailed Description

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Conditions

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Chronic Migraine, Headache

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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All participants

Previous treatment with onabotulinumtoxinA for Chronic Migraine based on retrospective review of medical records.

OnabotulinumtoxinA

Intervention Type BIOLOGICAL

Previous treatment with onabotulinumtoxinA for Chronic Migraine.

Interventions

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OnabotulinumtoxinA

Previous treatment with onabotulinumtoxinA for Chronic Migraine.

Intervention Type BIOLOGICAL

Other Intervention Names

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botulinum toxin Type A BOTOX®

Eligibility Criteria

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Inclusion Criteria

* History of chronic migraines
* 15 or more headache days over a 30 day period
* A minimum of 2 consecutive treatment cycles of 100 units onabotulinumtoxinA and a minimum of 2 consecutive treatment cycles with the onabotulinumtoxinA dosing between 155 and 195 units

Exclusion Criteria

* Any treatment cycle dose of onabotulinumtoxinA greater than 200 units
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Allergan

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Medical Director

Role: STUDY_DIRECTOR

Allergan

Other Identifiers

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GMA-BTX-CM-12-518

Identifier Type: -

Identifier Source: org_study_id

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